6957-91-1

Basic information

• Product Name: 4-aminobenzaldehyde thiosemicarbazone
• Synonyms: (2E)-2-(4-Aminobenzylidene)hydrazinecarbothioamide; Benzaldehyde, p-amino thiosemicarbazone; Hydrazinecarbothioamide, 2-((4-aminophenyl)methylene)-; hydrazinecarbothioamide, 2-[(4-aminophenyl)methylene]-, (2E)-
• CAS NO: 6957-91-1
• Molecular Formula: C₈H₁₀N₄S
• Molecular Weight: 194.2568
• Mol File: 6957-91-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 387.9°C at 760 mmHg
• Flash Point: 188.4°C
• Density: 1.34g/cm³
• Vapor Pressure: 3.18E-06mmHg at 25°C
• Refractive Index: 1.672
• CAS DataBase Reference: 4-aminobenzaldehyde thiosemicarbazone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-aminobenzaldehyde thiosemicarbazone(6957-91-1)
• EPA Substance Registry System: 4-aminobenzaldehyde thiosemicarbazone(6957-91-1)

Safety Data

• Hazardous Substances Data: 6957-91-1(Hazardous Substances Data)

Usage

General Description

4-aminobenzaldehyde thiosemicarbazone is a chemical compound that is commonly used in biochemical research and pharmaceutical applications. It is known for its ability to form complexes with various metal ions, making it a versatile ligand in metal ion coordination chemistry. 4-aminobenzaldehyde thiosemicarbazone also exhibits potential medicinal properties, with studies suggesting its antimicrobial and antitumor activities. Additionally, it has been studied for its potential use in treating diseases such as tuberculosis and malaria. Furthermore, 4-aminobenzaldehyde thiosemicarbazone has been investigated for its role as a chelating agent in environmental and industrial applications, such as in the removal of toxic metal ions from wastewater. Overall, this compound is a valuable and multifaceted chemical with diverse applications in both research and industry.

Upstream product

• 556-18-3 4-aminobenzaldehyde 
• 79-19-6 thiosemicarbazide 
• 4346-94-5 thiosemicarbazide hydrochloride 
• 5470-48-4 para-nitrobenzaldehyde thiosemicarbazone 

Downstream Products

• 100057-79-2 methoxy-acetic acid-(4-thiosemicarbazonomethyl-anilide) 
• 87896-45-5 propionic acid-(4-thiosemicarbazonomethyl-anilide) 
• 103754-57-0 (5Z)-5-(4-aminobenzylidene)-1,3-thiazolidine-2,4-dione 
• 61519-14-0 4-(N'-allyl-thioureido)-benzaldehyde-thiosemicarbazone 
• 51659-90-6 2-amino-5-(4-aminophenyl)-1,3,4-thiadiazole 
• 1338084-12-0 C₁₃H₁₀N₆O₂S 
• 1338084-00-6 C₁₅H₁₄N₆O₂S 
• 1338083-78-5 C₁₃H₁₁N₇O₂S 
• 1338084-33-5 C₁₈H₁₉N₇O₃S 
• 102943-72-6 4-(N'-methyl-thioureido)-benzaldehyde-thiosemicarbazone 
• 104-06-3 N-(4-[2-(aminocarbonothionyl)hydrazono]methylphenyl)acetamide 
• 92085-14-8 (4-thiosemicarbazonomethyl-anilino)-methanesulfonic acid 

Relevant articles and documents

Aryl thiosemicarbazones for the treatment of trypanosomatidic infections

Basing on a library of thiadiazole derivatives showing anti-trypanosomatidic activity, we have considered the thiadiazoles opened forms and reaction intermediates, thiosemicarbazones, as compounds of interest for phenotypic screening against Trypanosoma b

NEW PESTICIDES AND INTERMEDIATES. PART VII. SOME AZAALKENYL DERIVATIVES OF N-PHENYLUREA AND N-PHENYLCARBAMIC ACID

-